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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
1978 1
1987 1
1991 1
1993 1
1997 1
1998 1
1999 1
2000 2
2001 1
2002 3
2003 4
2004 5
2005 5
2006 5
2007 6
2008 5
2009 10
2010 17
2011 24
2012 29
2013 23
2014 12
2015 19
2016 10
2017 14
2018 9
2019 9
2020 4
2021 0
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Similar articles for PMID: 22144704

188 results
Results by year
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Page 1
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment.
Palka C, Alfonsi M, Mohn A, Cerbo R, Guanciali Franchi P, Fantasia D, Morizio E, Stuppia L, Calabrese G, Zori R, Chiarelli F, Palka G. Palka C, et al. Pediatrics. 2012 Jan;129(1):e183-8. doi: 10.1542/peds.2010-2094. Epub 2011 Dec 5. Pediatrics. 2012. PMID: 22144704
Phenotype of FOXP2 haploinsufficiency in a mother and son.
Rice GM, Raca G, Jakielski KJ, Laffin JJ, Iyama-Kurtycz CM, Hartley SL, Sprague RE, Heintzelman AT, Shriberg LD. Rice GM, et al. Am J Med Genet A. 2012 Jan;158A(1):174-81. doi: 10.1002/ajmg.a.34354. Epub 2011 Nov 21. Am J Med Genet A. 2012. PMID: 22106036 Free PMC article.
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.
Zeesman S, Nowaczyk MJ, Teshima I, Roberts W, Cardy JO, Brian J, Senman L, Feuk L, Osborne LR, Scherer SW. Zeesman S, et al. Am J Med Genet A. 2006 Mar 1;140(5):509-14. doi: 10.1002/ajmg.a.31110. Am J Med Genet A. 2006. PMID: 16470794
Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.
Lennon PA, Cooper ML, Peiffer DA, Gunderson KL, Patel A, Peters S, Cheung SW, Bacino CA. Lennon PA, et al. Am J Med Genet A. 2007 Apr 15;143A(8):791-8. doi: 10.1002/ajmg.a.31632. Am J Med Genet A. 2007. PMID: 17330859 Review.
Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.
Patel C, Cooper-Charles L, McMullan DJ, Walker JM, Davison V, Morton J. Patel C, et al. Eur J Hum Genet. 2011 Jun;19(6):634-9. doi: 10.1038/ejhg.2010.238. Epub 2011 Mar 9. Eur J Hum Genet. 2011. PMID: 21386874 Free PMC article.
De-novo balanced translocation between 7q31 and 10p14 in a girl with central precocious puberty, moderate mental retardation, and severe speech impairment.
Kosho T, Sakazume S, Kawame H, Wakui K, Wada T, Okoshi Y, Mikawa M, Hasegawa T, Matsuura N, Niikawa N, Matsumoto N, Fukushima Y. Kosho T, et al. Clin Dysmorphol. 2008 Jan;17(1):31-4. doi: 10.1097/MCD.0b013e3282f17688. Clin Dysmorphol. 2008. PMID: 18049078
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
Raca G, Baas BS, Kirmani S, Laffin JJ, Jackson CA, Strand EA, Jakielski KJ, Shriberg LD. Raca G, et al. Eur J Hum Genet. 2013 Apr;21(4):455-9. doi: 10.1038/ejhg.2012.165. Epub 2012 Aug 22. Eur J Hum Genet. 2013. PMID: 22909774 Free PMC article.
Genotype-phenotype relationship in a child with 2.3 Mb de novo interstitial 12p13.33-p13.32 deletion.
Fanizza I, Bertuzzo S, Beri S, Scalera E, Massagli A, Sali ME, Giorda R, Bonaglia MC. Fanizza I, et al. Eur J Med Genet. 2014 Jul;57(7):334-8. doi: 10.1016/j.ejmg.2014.04.009. Epub 2014 Apr 26. Eur J Med Genet. 2014. PMID: 24780630
Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH.
Tyson C, McGillivray B, Chijiwa C, Rajcan-Separovic E. Tyson C, et al. Am J Med Genet A. 2004 Sep 1;129A(3):254-60. doi: 10.1002/ajmg.a.30245. Am J Med Genet A. 2004. PMID: 15326624
Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization.
Laffin JJ, Raca G, Jackson CA, Strand EA, Jakielski KJ, Shriberg LD. Laffin JJ, et al. Genet Med. 2012 Nov;14(11):928-36. doi: 10.1038/gim.2012.72. Epub 2012 Jul 5. Genet Med. 2012. PMID: 22766611 Free PMC article.
188 results
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